EP2499181B1 - Polymer für ein optoelektronisches bauelement - Google Patents

Polymer für ein optoelektronisches bauelement Download PDF

Info

Publication number
EP2499181B1
EP2499181B1 EP10754636.8A EP10754636A EP2499181B1 EP 2499181 B1 EP2499181 B1 EP 2499181B1 EP 10754636 A EP10754636 A EP 10754636A EP 2499181 B1 EP2499181 B1 EP 2499181B1
Authority
EP
European Patent Office
Prior art keywords
polymer
structural unit
optoelectronic device
radical
independently
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP10754636.8A
Other languages
English (en)
French (fr)
Other versions
EP2499181A1 (de
Inventor
Qing Ye
Jie Liu
Kelly Scott Chichak
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BOE Technology Group Co Ltd
Original Assignee
BOE Technology Group Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BOE Technology Group Co Ltd filed Critical BOE Technology Group Co Ltd
Publication of EP2499181A1 publication Critical patent/EP2499181A1/de
Application granted granted Critical
Publication of EP2499181B1 publication Critical patent/EP2499181B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C08G73/026—Wholly aromatic polyamines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/12—Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10—Organic polymers or oligomers
    • H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/142—Side-chains containing oxygen
    • C08G2261/1424—Side-chains containing oxygen containing ether groups, including alkoxy
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/148—Side-chains having aromatic units
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/149—Side-chains having heteroaromatic units
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/152—Side-groups comprising metal complexes
    • C08G2261/1526—Side-groups comprising metal complexes of Os, Ir, Pt, Ru, Rh or Pd
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • C08G2261/314—Condensed aromatic systems, e.g. perylene, anthracene or pyrene
    • C08G2261/3142—Condensed aromatic systems, e.g. perylene, anthracene or pyrene fluorene-based, e.g. fluorene, indenofluorene, or spirobifluorene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • C08G2261/316—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain bridged by heteroatoms, e.g. N, P, Si or B
    • C08G2261/3162—Arylamines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/40—Polymerisation processes
    • C08G2261/41—Organometallic coupling reactions
    • C08G2261/411—Suzuki reactions
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/50—Physical properties
    • C08G2261/52—Luminescence
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1416—Condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1425—Non-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1433—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1441—Heterocyclic
    • C09K2211/1466—Heterocyclic containing nitrogen as the only heteroatom
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/18—Metal complexes
    • C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd

Definitions

  • the invention relates generally to polymers useful, e.g., in light emissive layers of optoelectronic devices, and the optoelectronic devices comprising the polymers.
  • Optoelectronic devices e.g. Organic Light Emitting Devices (OLEDs), which make use of thin film materials that emit light when subjected to a voltage bias, are expected to become an increasingly popular form of flat panel display technology.
  • OLEDs have a wide variety of potential applications, including cell phones, personal digital assistants (PDAs), computer displays, informational displays in vehicles, television monitors, as well as light sources for general illumination. Due to their bright colors, wide viewing angle, compatibility with full motion video, broad temperature ranges, thin and conformable form factor, low power requirements and the potential for low cost manufacturing processes, OLEDs are seen as a future replacement technology for cathode ray tubes (CRTs) and liquid crystal displays (LCDs). Due to their high luminous efficiencies, OLEDs are seen as having the potential to replace incandescent, and perhaps even fluorescent, lamps for certain types of applications.
  • CTRs cathode ray tubes
  • LCDs liquid crystal displays
  • OLEDs possess a sandwiched structure, which consists of one or more organic layers between two opposite electrodes.
  • multi-layered devices usually comprise at least three layers: a hole injection/transport layer, an emissive layer and an electron transport layer (ETL).
  • the hole injection/transport layer serves as an electron blocking layer and the ETL as a hole blocking layer.
  • Single-layered OLEDs comprise only one layer of materials between two opposite electrodes.
  • WO 2009/079039A1 discloses polymers prepared from monomers which include a fluorene with pendant iridium complex, a further aryl monomer unit and a further structural unit derived from a triarylamine.
  • US2008026477A1 provides polymeric organic iridium compositions comprising at least one cyclometallated ligand and at least one ketopyrrole ligand.
  • WO2008014037A2 provides compositions comprising at least one novel organic iridium compound which comprises at least one cyclometallated ligand and at least one ketopyrrole ligand.
  • the invention relates to a polymer comprising structural unit of formula I: wherein
  • the invention relates to an optoelectronic device comprising the above polymer.
  • the invention relates to a polymer comprising structural unit of formula I: wherein
  • the invention relates to an optoelectronic device comprising the above polymer.
  • L is derived from phenylisoquinoline.
  • the polymer comprises structural unit of formula II II, wherein
  • the polymer comprises structural units of formula III
  • the polymer comprises structural units derived from and
  • the polymer comprises structural units derived from
  • the polymer comprises structural units derived from
  • the polymer comprises structural units derived from
  • the polymers are made by processes comprising Suzuki cross-coupling reactions in a suitable solvent, in the presence of a base and Pd catalyst.
  • the reaction mixture is heated under an inert atmosphere for a period of time.
  • Suitable solvents include but are not limited to dioxane, THF, EtOH, toluene and mixtures thereof.
  • Exemplary bases include KOAc, Na 2 CO 3 , K 2 CO 3 , Cs 2 CO 3 , potassium phosphate and hydrates thereof.
  • the bases can be added to the reaction as a solid powder or as an aqueous solution.
  • the most commonly used catalysts include Pd(PPh 3 ) 4 , Pd 2 (dba) 3 , or Pd(OAc) 2 , Pd(dba) 2 with the addition of a secondary ligand.
  • exemplary ligands include dialkylphosphinobiphenyl ligands, such as structures V-IX shown below, in which Cy is cyclohexyl.
  • the polymerization reaction is conducted for a time period necessary to achieve a polymer of a suitable molecular weight.
  • the molecular weights of a polymer is determined by any of the techniques known to those skilled in the art, and include viscosity measurements, light scattering, and osmometry.
  • the molecular weight of a polymer is typically represented as a number average molecular weight Mn, or weight average molecular weight, Mw.
  • a particularly useful technique to determine molecular weight averages is gel permeation chromatography (GPC), from which both number average and weight average molecular weights are obtained.
  • polymers of Mw greater than 30,000 grams per mole (g/mol) are desirable, in other embodiments, polymers of Mw greater than 50,000 g/mol are desirable, while in yet other embodiments, polymer of Mw greater than 80,000 g/mol are desirable.
  • the polymer has a highest occupied molecular orbital (HOMO) of 4.8 eV.
  • the polymer comprises both hole transport moiety and light emissive moiety and is insoluble in solvents subsequently applied in forming multi-layer optoelectronic devices using wet-coating or printing processes.
  • the polymer is usable for example in white OLEDs which are fabricated by wet-coating or printing processes and which have more than one light emissive layers.
  • the polymer is usable in at least one of the more than one light emissive layers of the white OLEDs.
  • An optoelectronic device typically includes in the simplest case, an anode layer and a corresponding cathode layer with an organic electroluminescent layer disposed between said anode and said cathode.
  • an OLED typically includes in the simplest case, an anode layer and a corresponding cathode layer with an organic electroluminescent layer disposed between said anode and said cathode.
  • a voltage bias is applied across the electrodes, electrons are injected by the cathode into the electroluminescent layer while electrons are removed from (or "holes" are “injected” into) the electroluminescent layer from the anode.
  • Light emission occurs as holes combine with electrons within the electroluminescent layer to form singlet or triplet excitons, light emission occurring as singlet and/or triplet excitons decay to their ground states via radiative decay.
  • Other components which may be present in an OLED in addition to the anode, cathode and light emitting material include a hole injection layer, an electron injection layer, and an electron transport layer.
  • the electron transport layer need not be in direct contact with the cathode, and frequently the electron transport layer also serves as a hole blocking layer to prevent holes migrating toward the cathode.
  • Additional components which may be present in an organic light-emitting device include hole transporting layers, hole transporting emission (emitting) layers and electron transporting emission (emitting) layers.
  • the OLEDs comprising the polymers of the invention may be a fluorescent OLED comprising a singlet emitter.
  • the OLEDs comprising the polymers of the invention may be a phosphorescent OLED comprising at least one triplet emitter.
  • the OLEDs comprising the polymers of the invention comprise at least one singlet emitter and at least one triplet emitter.
  • the OLEDs comprising the polymers of the invention may contain one or more, any or a combination of blue, yellow, orange, red phosphorescent dyes, including complexes of transition metals such as Ir, Os and Pt.
  • electrophosphorescent and electrofluorescent metal complexes such as those supplied by American Dye Source, Inc., Quebec, Canada may be used.
  • Polymers comprising structural unit of any of formula I to IV may be part of an emissive layer, or hole transporting layer or electron transporting layer, or electron injection layer of an OLED or any combination thereof.
  • the organic electroluminescent layer i.e., the emissive layer
  • the organic electroluminescent layer is a layer within an organic light emitting device which when in operation contains a significant concentration of both electrons and holes and provides sites for exciton formation and light emission.
  • a hole injection layer is a layer in contact with the anode which promotes the injection of holes from the anode into the interior layers of the OLED; and an electron injection layer is a layer in contact with the cathode that promotes the injection of electrons from the cathode into the OLED;
  • an electron transport layer is a layer which facilitates conduction of electrons from the cathode and/or the electron injection layer to a charge recombination site.
  • a hole transporting layer is a layer which when the OLED is in operation facilitates conduction of holes from the anode and/or the hole injection layer to charge recombination sites and which need not be in direct contact with the anode.
  • a hole transporting emission layer is a layer in which when the OLED is in operation facilitates the conduction of holes to charge recombination sites, and in which the majority of charge carriers are holes, and in which emission occurs not only through recombination with residual electrons, but also through the transfer of energy from a charge recombination zone elsewhere in the device.
  • An electron transporting emission layer is a layer in which when the OLED is in operation facilitates the conduction of electrons to charge recombination sites, and in which the majority of charge carriers are electrons, and in which emission occurs not only through recombination with residual holes, but also through the transfer of energy from a charge recombination zone elsewhere in the device.
  • Materials suitable for use as the anode includes materials having a bulk resistivity of preferred about 1000 ohms per square, as measured by a four-point probe technique.
  • Indium tin oxide (ITO) is frequently used as the anode because it is substantially transparent to light transmission and thus facilitates the escape of light emitted from electro-active organic layer.
  • Other materials, which may be utilized as the anode layer include tin oxide, indium oxide, zinc oxide, indium zinc oxide, zinc indium tin oxide, antimony oxide, and mixtures thereof.
  • Materials suitable for use as the cathode include general electrical conductors including, but not limited to metals and metal oxides such as ITO etc which can inject negative charge carriers (electrons) into the inner layer(s) of the OLED.
  • Various metals suitable for use as the cathode include K, Li, Na, Cs, Mg, Ca, Sr, Ba, Al, Ag, Au, In, Sn, Zn, Zr, Sc, Y, elements of the lanthanide series, alloys thereof, and mixtures thereof.
  • Suitable alloy materials for use as the cathode layer include Ag-Mg, Al-Li, In-Mg, Al-Ca, and Al-Au alloys.
  • Layered non-alloy structures may also be employed in the cathode, such as a thin layer of a metal such as calcium, or a metal fluoride, such as LiF, covered by a thicker layer of a metal, such as aluminum or silver.
  • the cathode may be composed of a single metal, and especially of aluminum metal.
  • Materials suitable for use in electron transport layers include poly(9,9-dioctyl fluorene), tris(8-hydroxyquinolato) aluminum (Alq 3 ), 2,9-dimethyl-4,7-diphenyl-1,1-phenanthroline, 4,7-diphenyl-1,10-phenanthroline, 2-(4-biphenylyl)-5-(4-t-butylphenyl)-1,3,4-oxadiazole, 3-(4-biphenylyl)-4-phenyl-5-(4-t-butylphenyl)-1,2,4- triazole, 1,3,4-oxadiazole-containing polymers, 1,3,4-triazole-containing polymers, quinoxaline-containing polymers, and cyano-PPV.
  • Materials suitable for use in hole transporting layers include such as 1,1-bis((di-4-tolylamino) phenyl)cyclohexane, N,N'- bis(4-methylphenyl)-N,N'-bis(4-ethylphenyl)-(1,1'-(3,3'-dimethyl)biphenyl)-4,4'-diamine, tetrakis-(3-methylphenyl)-N,N,N',N'-2,5-phenylenediamine, phenyl-4-N,N-diphenylaminostyrene, p-(diethylamino) benzaldehyde diphenylhydrazone, triphenylamine, 1-phenyl-3-(p-(diethylamino)styryl)-5-(p-(diethylamino)phenyl)pyrazoline, 1,2-trans-bis(9H-carbazol-9-yl)cyclobutan
  • Polymers comprising structural units of any of formula I to IV may be used in the light emitting layer in place of, or in addition to traditional electroluminescent polymers such as polyfluorenes, preferably poly(9,9-dioctyl fluorene) and copolymers thereof, such as poly(9,9'-dioctylfluorene- co -bis- N,N '-(4-butylphenyl)diphenylamine) (F8-TFB); poly(vinylcarbazole) and polyphenylenevinylene and their derivatives.
  • the light emitting layer may include a blue, yellow, orange, green or red phosphorescent dye or metal complex, or a combination thereof.
  • Materials suitable for use as the phosphorescent dye include, but are not limited to, tris(1-phenylisoquinoline) iridium (III) (red dye), tris(2-phenylpyridine) iridium (green dye) and Iridium (III) bis(2-(4,6-difluorephenyl)pyridinato-N,C2) (blue dye).
  • commercially available electrofluorescent and electrophosphorescent metal complexes from ADS may also be used.
  • ADS green dyes include ADS060GE, ADS061GE, ADS063GE, and ADS066GE, ADS078GE, and ADS090GE.
  • ADS blue dyes include ADS064BE, ADS065BE, and ADS070BE.
  • ADS red dyes include ADS067RE, ADS068RE, ADS069RE, ADS075RE, ADS076RE, ADS067RE, and ADS077RE.
  • Polymers comprising structural unit of any of formula I to IV may form part of the hole transport layer or hole injection layer or light emissive layer of optoelectronic devices, e.g., OLEDs.
  • OLEDs may be phosphorescent containing one or more, any or a combination of, blue, yellow, orange, green, red phosphorescent dyes.
  • aromatic radical refers to an array of atoms having a valence of at least one comprising at least one aromatic group.
  • the array of atoms having a valence of at least one comprising at least one aromatic group may include heteroatoms such as nitrogen, sulfur, selenium, silicon and oxygen, or may be composed exclusively of carbon and hydrogen.
  • aromatic radical includes but is not limited to phenyl, pyridyl, furanyl, thienyl, naphthyl, phenylene, and biphenyl radicals.
  • the aromatic radical contains at least one aromatic group.
  • the aromatic radical may also include nonaromatic components.
  • a benzyl group is an aromatic radical which comprises a phenyl ring (the aromatic group) and a methylene group (the nonaromatic component).
  • a tetrahydronaphthyl radical is an aromatic radical comprising an aromatic group (C 6 H 3 ) fused to a nonaromatic component -(CH 2 ) 4 -.
  • aromatic radical is defined herein to encompass a wide range of functional groups such as alkyl groups, alkenyl groups, alkynyl groups, haloalkyl groups, haloaromatic groups, conjugated dienyl groups, alcohol groups, ether groups, aldehydes groups, ketone groups, carboxylic acid groups, acyl groups (for example carboxylic acid derivatives such as esters and amides), amine groups, nitro groups, and the like.
  • the 4-methylphenyl radical is a C 7 aromatic radical comprising a methyl group, the methyl group being a functional group which is an alkyl group.
  • the 2-nitrophenyl group is a C 6 aromatic radical comprising a nitro group, the nitro group being a functional group.
  • Aromatic radicals include halogenated aromatic radicals such as 4-trifluoromethylphenyl, hexafluoroisopropylidenebis(4-phen-1-yloxy) (i.e., -OPhC(CF 3 ) 2 PhO-), 4-chloromethylphen-1-yl, 3-trifluorovinyl-2-thienyl, 3-trichloromethylphen-1-yl (i.e., 3-CCl 3 Ph-), 4-(3-bromoprop-1-yl)phen-1-yl (i.e., 4-BrCH 2 CH 2 CH 2 Ph-), and the like.
  • halogenated aromatic radicals such as 4-trifluoromethylphenyl, hexafluoroisopropylidenebis(4-phen-1-yloxy) (i.e., -OPhC(CF 3 ) 2 PhO-), 4-chloromethylphen-1-yl, 3-trifluorovinyl-2-thienyl, 3-trich
  • aromatic radicals include 4-allyloxyphen-1-oxy, 4-aminophen-1-yl (i.e., 4-H 2 NPh-), 3-aminocarbonylphen-1-yl (i.e., NH 2 COPh-), 4-benzoylphen-1-yl, dicyanomethylidenebis(4-phen-1-yloxy) (i.e., -OPhC(CN) 2 PhO-), 3-methylphen-1-yl, methylenebis(4-phen-1-yloxy) (i.e.,-OPhCH 2 PhO-), 2-ethylphen-1-yl, phenylethenyl, 3-formyl-2-thienyl, 2-hexyl-5-furanyl, hexamethylene-1,6-bis(4-phen-1-yloxy) (i.e., -OPh(CH 2 ) 6 PhO-), 4-hydroxymethylphen-1-yl (i.e., 4-HOCH 2 Ph-), 4-mercap
  • a C 3 - C 20 aromatic radical includes aromatic radicals containing at least three but no more than 20 carbon atoms.
  • the aromatic radical 1-imidazolyl (C 3 H 2 N 2 -) represents a C 3 aromatic radical.
  • the benzyl radical (C 7 H 7 -) represents a C 7 aromatic radical.
  • cycloaliphatic radical refers to a radical having a valence of at least one, and comprising an array of atoms which is cyclic but which is not aromatic. As defined herein a “cycloaliphatic radical” does not contain an aromatic group.
  • a "cycloaliphatic radical” may comprise one or more noncyclic components.
  • a cyclohexylmethyl group (C 6 H 11 CH 2 -) is an cycloaliphatic radical which comprises a cyclohexyl ring (the array of atoms which is cyclic but which is not aromatic) and a methylene group (the noncyclic component).
  • the cycloaliphatic radical may include heteroatoms such as nitrogen, sulfur, selenium, silicon and oxygen, or may be composed exclusively of carbon and hydrogen.
  • cycloaliphatic radical is defined herein to encompass a wide range of functional groups such as alkyl groups, alkenyl groups, alkynyl groups, haloalkyl groups, conjugated dienyl groups, alcohol groups, ether groups, aldehyde groups, ketone groups, carboxylic acid groups, acyl groups (for example carboxylic acid derivatives such as esters and amides), amine groups, nitro groups, and the like.
  • the 4-methylcyclopent-1-yl radical is a C 6 cycloaliphatic radical comprising a methyl group, the methyl group being a functional group which is an alkyl group.
  • the 2-nitrocyclobut-1-yl radical is a C 4 cycloaliphatic radical comprising a nitro group, the nitro group being a functional group.
  • a cycloaliphatic radical may comprise one or more halogen atoms which may be the same or different. Halogen atoms include, for example; fluorine, chlorine, bromine, and iodine.
  • Cycloaliphatic radicals comprising one or more halogen atoms include 2-trifluoromethylcyclohex-1-yl, 4-bromodifluoromethylcyclooct-1-yl, 2-chlorodifluoromethylcyclohex-1-yl, hexafluoroisopropylidene-2,2-bis (cyclohex-4-yl) (i.e., -C 6 H 10 C(CF 3 ) 2 C 6 H 10 -), 2-chloromethylcyclohex-1-yl, 3-difluoromethylenecyclohex-1-yl, 4-trichloromethylcyclohex-1-yloxy, 4-bromodichloromethylcyclohex-1-ylthio, 2-bromoethylcyclopent-1-yl, 2-bromopropylcyclohex-1-yloxy (e.g.
  • cycloaliphatic radicals include 4-allyloxycyclohex-1-yl, 4-aminocyclohex-1-yl (i.e., H 2 NC 6 H 10 -), 4-aminocarbonylcyclopent-1-yl (i.e., NH 2 COC 5 H 8 -), 4-acetyloxycyclohex-1-yl, 2,2-dicyanoisopropylidenebis(cyclohex-4-yloxy) (i.e., -OC 6 H 10 C(CN) 2 C 6 H 10 O-), 3-methylcyclohex-1-yl, methylenebis(cyclohex-4-yloxy) (i.e., -OC 6 H 10 CH 2 C 6 H 10 O-), 1-ethylcyclobut-1-yl, cyclopropylethenyl, 3-formyl-2-terahydrofuranyl, 2-hexyl-5
  • a C 3 - C 10 cycloaliphatic radical includes cycloaliphatic radicals containing at least three but no more than 10 carbon atoms.
  • the cycloaliphatic radical 2-tetrahydrofuranyl (C 4 H 7 O-) represents a C 4 cycloaliphatic radical.
  • the cyclohexylmethyl radical (C 6 H 11 CH 2 -) represents a C 7 cycloaliphatic radical.
  • aliphatic radical refers to an organic radical having a valence of at least one consisting of a linear or branched array of atoms which is not cyclic. Aliphatic radicals are defined to comprise at least one carbon atom. The array of atoms comprising the aliphatic radical may include heteroatoms such as nitrogen, sulfur, silicon, selenium and oxygen or may be composed exclusively of carbon and hydrogen.
  • aliphatic radical is defined herein to encompass, as part of the "linear or branched array of atoms which is not cyclic" organic radicals substituted with a wide range of functional groups such as alkyl groups, alkenyl groups, alkynyl groups, haloalkyl groups, conjugated dienyl groups, alcohol groups, ether groups, aldehyde groups, ketone groups, carboxylic acid groups, acyl groups (for example carboxylic acid derivatives such as esters and amides), amine groups, nitro groups, and the like.
  • functional groups such as alkyl groups, alkenyl groups, alkynyl groups, haloalkyl groups, conjugated dienyl groups, alcohol groups, ether groups, aldehyde groups, ketone groups, carboxylic acid groups, acyl groups (for example carboxylic acid derivatives such as esters and amides), amine groups, nitro groups, and the like.
  • the 4-methylpent-1-yl radical is a C 6 aliphatic radical comprising a methyl group, the methyl group being a functional group which is an alkyl group.
  • the 4-nitrobut-1-yl group is a C 4 aliphatic radical comprising a nitro group, the nitro group being a functional group.
  • An aliphatic radical may be a haloalkyl group which comprises one or more halogen atoms which may be the same or different. Halogen atoms include, for example; fluorine, chlorine, bromine, and iodine.
  • Aliphatic radicals comprising one or more halogen atoms include the alkyl halides trifluoromethyl, bromodifluoromethyl, chlorodifluoromethyl, hexafluoroisopropylidene, chloromethyl, difluorovinylidene, trichloromethyl, bromodichloromethyl, bromoethyl, 2-bromotrimethylene (e.g.-CH 2 CHBrCH 2 -), and the like.
  • aliphatic radicals include allyl, aminocarbonyl (i.e., -CONH 2 ), carbonyl, 2,2-dicyanoisopropylidene (i.e.,-CH 2 C(CN) 2 CH 2 -), methyl (i.e., -CH 3 ), methylene (i.e., -CH 2 -), ethyl, ethylene, formyl (i.e.-CHO), hexyl, hexamethylene, hydroxymethyl (i.e.-CH 2 OH), mercaptomethyl (i.e., -CH 2 SH), methylthio (i.e., -SCH 3 ), methylthiomethyl (i.e., -CH 2 SCH 3 ), methoxy, methoxycarbonyl (i.e., CH 3 OCO-), nitromethyl (i.e., -CH 2 NO 2 ), thiocarbonyl, trimethylsilyl (i.e., (CHCH 2
  • a C 1 - C 20 aliphatic radical contains at least one but no more than 20 carbon atoms.
  • a methyl group i.e., CH 3 -
  • a decyl group i.e., CH 3 (CH 2 ) 9 -
  • CH 3 (CH 2 ) 9 - is an example of a C 10 aliphatic radical.
  • heteroaryl refers to aromatic or unsaturated rings in which one or more carbon atoms of the aromatic ring(s) are replaced by a heteroatom(s) such as nitrogen, oxygen, boron, selenium, phosphorus, silicon or sulfur.
  • Heteroaryl refers to structures that may be a single aromatic ring, multiple aromatic ring(s), or one or more aromatic rings coupled to one or more non-aromatic ring(s). In structures having multiple rings, the rings can be fused together, linked covalently, or linked to a common group such as an ether, methylene or ethylene moiety.
  • the common linking group may also be a carbonyl as in phenyl pyridyl ketone.
  • heteroaryl rings include thiophene, pyridine, isoxazole, pyrazole, pyrrole, furan, imidazole, indole, thiazole, benzimidazole, quinoline, isoquinoline, quinoxaline, pyrimidine, pyrazine, tetrazole, triazole, benzo-fused analogues of these groups, benzopyranone, phenylpyridine, tolylpyridine, benzothienylpyridine, phenylisoquinoline, dibenzoquinozaline, fluorenylpyridine, ketopyrrole, 2-phenylbenzoxazole, 2 phenylbenzothiazole, thienylpyridine, benzothienylpyridine, 3 methoxy-2-phenylpyridine, phenylimine, pyridylnaphthalene, pyridylpyrrole, pyridylimidazole, and
  • aryl is used herein to refer to an aromatic substituent which may be a single aromatic ring or multiple aromatic rings which are fused together, linked covalently, or linked to a common group such as an ether, methylene or ethylene moiety.
  • the aromatic ring(s) may include phenyl, naphthyl, anthracenyl, and biphenyl, among others.
  • aryls have between 1 and 200 carbon atoms, between 1 and 50 carbon atoms or between 1 and 20 carbon atoms.
  • alkyl is used herein to refer to a branched or unbranched, saturated or unsaturated acyclic hydrocarbon radical. Suitable alkyl radicals include, for example, methyl, ethyl, n-propyl, i-propyl, 2-propenyl (or allyl), vinyl, n-butyl, t-butyl, i-butyl (or 2-methylpropyl), etc. In particular embodiments, alkyls have between 1 and 200 carbon atoms, between 1 and 50 carbon atoms or between 1 and 20 carbon atoms.
  • cycloalkyl is used herein to refer to a saturated or unsaturated cyclic non-aromatic hydrocarbon radical having a single ring or multiple condensed rings.
  • Suitable cycloalkyl radicals include, for example, cyclopentyl, cyclohexyl, cyclooctenyl, bicyclooctyl, etc.
  • cycloalkyls have between 3 and 200 carbon atoms, between 3 and 50 carbon atoms or between 3 and 20 carbon atoms.
  • any numerical values recited herein include all values from the lower value to the upper value in increments of one unit provided that there is a separation of at least 2 units between any lower value and any higher value.
  • the amount of a component or a value of a process variable such as, for example, temperature, pressure, time and the like is, for example, from 1 to 90, preferably from 20 to 80, more preferably from 30 to 70, it is intended that values such as 15 to 85, 22 to 68, 43 to 51, 30 to 32 etc. are expressly enumerated in this specification.
  • one unit is considered to be 0.0001, 0.001, 0.01 or 0.1 as appropriate.
  • N-Butyl aniline (50 g, 0.34 mol) was dissolved in 90 mL of AcOH under ice cooling.
  • Ac 2 O 40 mL was added drop wise to ensure that the temperature did not exceed 30 °C.
  • the reaction mixture was then heated at 40 °C for 1.5 hours.
  • the mixture was cooled to room temperature and poured into H 2 O (500 mL) to precipitate.
  • the precipitated solid was collected by filtration and dried in a vacuum oven.
  • the solid was crystallized from toluene (60 mL) / hexane (500 mL) to give colorless plates (60.1 g).
  • the reaction mixture was cooled and diluted with CH 2 Cl 2 and filtered.
  • the filter cake was washed with CH 2 Cl 2 and the filtrate was concentrated to dryness to give a green oil.
  • the crude solid was dissolved in EtOAc/CH 2 Cl 2 and passed through a 30 cm ⁇ 10 cm column of SiO 2 .
  • the combined fractions were concentrated to dryness and the solid was crystallized twice from EtOAc and carried on to the next step without further purification (29.6 g).
  • the progress of the reaction was monitored by TLC (10% CH 2 Cl 2 /hexane) and after 4 hours TLC indicated that the reaction was complete.
  • the reaction mixture was then cooled to room temperature and diluted with EtOAc and treated with mercapto-functionalized SiO 2 (4.0 g) and stirred for 45 minutes.
  • the mixture was then filtered through a bed of celite and washed with EtOAc.
  • the filtrate was adsorbed onto SiO 2 and chromatographed through SiO 2 (10% CH 2 Cl 2 /Hexanes) to give a white foam (dimer-bromide monomer, 12.6 g).
  • a flame dried flask was placed under an atmosphere of nitrogen and was charged with the dimer-bromide monomer (10.0 g, 13.2 mmol), bis-pinacolatodiborane (10.0 g, 39.5 mmol), anhydrous KOAc (4.0 g, 39.5 mmol), Pd(OAc) 2 (65.8 mg, 0.29 mmol), and the cyclohexylphoshine ligand (263 mg, 0.64 mmol).
  • anhydrous THF 75 mL
  • the stirred solution was purged with nitrogen for 10 minutes and then heated at reflux until TLC (CH 2 Cl 2 /hexane) indicated that the starting dimer-bromide monomer no longer remained.
  • reaction mixture was cooled to room temperature and diluted with an equal volume of CH 2 Cl 2 /hexane (1:1), filtered through a bed of celite, washed with CH 2 Cl 2 /hexane, and the filtrate was concentrated to dryness. The residue was chromatographed through SiO 2 eluting with CH 2 Cl 2 /hexane (1:1) to give 4.8 g of an off-white foam (dimer-bis borate monomer).
  • Bromo-(4-hexyloxy)-benzene was prepared by alkylation of 4-bromophenol (91.2 g, 527 mmol) with bromohexane (86.0 g, 520 mmol), K 2 CO 3 (80.0 g, 580 mmol) in acetone (200 mL) at relfux for 12 hours. After removal of the salts by filtration, the reaction mixture was concentrated to dryness to give an oil. The oil was dissolved in EtOAc (100 mL) and transferred to a separatory funnel and washed with 5% NaOH (4 ⁇ 200 mL).
  • the cooling bath was removed and the reaction was stirred for an additional 10 minutes as the temperature of the reaction rose to 28°C.
  • the reaction was cooled to room temperature and the contents were transferred by pipette to a stirred toluene (250 mL) suspension of 2,7,-dibromofluorenone (30.0 g, 90.4 mmol) that was maintained at -10 °C with a cooling bath.
  • the cooling bath was removed and the reaction mixture was stirred at room temperature for 20 minutes and subsequently treated with 20 mL of EtOH and a saturated solution of NH 4 Cl (5 mL).
  • the reaction mixture was filtered to remove insoluble materials and transferred to a separatory funnel containing EtOAc (100 mL) and H 2 O (100 mL).
  • the oil was adsorbed onto silica gel from a CH 2 Cl 2 solution and the solvents were removed to dryness.
  • the dried silica gel was transferred to the top of a glass fritted funnel (500 mL) containing a packed H 2 O slurry of silica gel (200 mL) fitted on top of a vacuum flask.
  • the contents of the funnel were flushed with H 2 O by applying vacuum to the flask which eluted phenol from the silica gel.
  • the product was eluted from the silica gel with CH 3 CN.
  • the solvents were removed using a rotary evaporator with a bath at 45 °C which resulted in the formation of a milky solution from which a white solid formed.
  • the 9-(4-Hexyloxyphenyl)-9'-(4-hydroxyphenyl)-fluorene (33.0 g, 53.7 mmol) was dissolved in xylene (30 mL), dried over MgSO 4 , and filtered. The solution was concentrated on a rotary evaporator until the contents of the flask weighed 70 g. The xylene solution of 9-(4-Hexyloxyphenyl)-9'-(4-hydroxyphenyl)-fluorene was then placed under an inert atmosphere of nitrogen and treated with ethylene carbonate (3.9 mL, 59.0 mmol) which was then heated at reflux for 15 hours.
  • a toluene solution (200 mL) of the ethylene glycol (9-(4-Hexyloxyphenyl)-9'-(4-(2-hydroxyethoxy)phenyl)-fluorene) (29.1 g, 44.2 mmol) was treated with p- toluenesulfonyl chloride (13.3 g, 69.8 mmol) and triethyamine (19.4 mL, 140 mmol) and stirred at room temperature for 60 hours under an inert atmosphere of nitrogen. The reaction mixture was then filtered to remove triethylamine hydrochloride and concentrated to dryness.
  • Ligand 1 was recrystalized from acetone before use. All monomers were dried at 50 °C in a vacuum oven for at least 2 hours prior to weighing.
  • the ligand 1 is 2-dicyclohexylphosphino-2',6'-dimethoxy-biphenyl, Aldrich No. 638072, with structure below.
  • the flask was then immersed in a 75 °C oil bath. Stirring and heating under a positive argon pressure for 24-48 hours.
  • the warm polymer solution was dropwise added into 3 times of volume of acetone solution under rapid stirring. The solution was left still before the supernant was decanted away and the residue was transferred to centrifuge tubes while wrapped in aluminum foil. After centrifugation, the tubes were transferred into the nitrogen purge box to decant away the solvent.
  • the isolated powder was transferred to a vial and re-dissolved in hot toluene ( ⁇ 0.5 g polymer used about 15-20 mL of toluene). Then to this solution 4 fold amount of amine-functionalized silica gel was added and stirred on a hot plate at 70-90 °C to keep the polymer in solution for 1 hour. The solution was filtered through a fluted filter paper.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Materials Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Electroluminescent Light Sources (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Claims (18)

  1. Polymer aufweisend Struktureinheiten der Formel I:
    Figure imgb0044
     worin
    R1 unabhängig bei jedem Auftreten eine aliphatische C1-C20-Gruppe, eine aromatische C3-C20-Gruppe oder eine cycloaliphatische C3-C20-Gruppe ist;
    a unabhängig bei jedem Auftreten eine ganze Zahl im Bereich von 0 bis 4 ist; Ar1 ausgewählt ist aus
    Figure imgb0045
    Ar2 Fluoren ist;
    R2 Alkylen, substituiertes Alkylen, Oxaalkylen, CO oder CO2 ist;
    R3, R4 und R5 unabhängig Wasserstoff, Alkyl, Alkoxy, Alkylaryl, Aryl, Arylalkyl, Heteroaryl, substituiertes Alkyl, substituiertes Alkoxy, substituiertes Alkylaryl, substituiertes Aryl, substituiertes Arylalkyl oder substituiertes Heteroaryl sind; und
    L abgeleitet ist von Phenylpyridin, Tolylpyridin, Benzothienylpyridin, Phenylisochinolin, Dibenzochinozalin, Fluorenylpyridin, Ketopyrrol, 2-(1-Naphthyl)benzoxazol)), 2-Phenylbenzoxazol, 2-Phenylbenzothiazol, Cumarin, Thienylpyridin, Phenylpyridin, Benzothienylpyridin, 3-Methoxy-2-phenylpyridin, Thienylpyridin, Phenylimin, Vinylpyridin, Pyridylnaphthalen, Pyridylpyrrol, Pyridylimidazol, Phenylindol, Derivaten davon oder Kombinationen davon.
  2. Polymer nach Anspruch 1, wobei sich Ar2 von einem Dibrom-9,9-dioctyl-fluoren-Monomer ableitet.
  3. Polymer nach Anspruch 1, wobei L von Phenylisochinolin abgeleitet ist.
  4. Polymer nach Anspruch 1, aufweisend Struktureinheiten der Formel II
    Figure imgb0046
     worin
    R6 und R7 unabhängig bei jedem Auftreten eine aliphatische C1-C20-Gruppe, eine aromatische C3-C20-Gruppe oder eine cycloaliphatische C3-C20-Gruppe sind;
    b unabhängig bei jedem Auftreten eine ganze Zahl im Bereich von 0-3 ist; und
    c unabhängig bei jedem Auftreten eine ganze Zahl im Bereich von 0-2 ist.
  5. Polymer nach Anspruch 1, aufweisend Struktureinheiten der Formel III
    Figure imgb0047
  6. Polymer nach Anspruch 1, aufweisend Struktureinheiten der Formel IV
    Figure imgb0048
     worin x+y=100.
  7. Polymer nach Anspruch 1, aufweisend Struktureinheiten, die abgeleitet sind von
    Figure imgb0049
     und
    Figure imgb0050
  8. Optoelektronische Vorrichtung aufweisend ein Polymer nach Anspruch 1.
  9. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten der Formel II aufweist
    Figure imgb0051
     worin
    R6 und R7 unabhängig bei jedem Auftreten eine aliphatische C1-C20-Gruppe, eine aromatische C3-C20-Gruppe oder eine cycloaliphatische C3-C20-Gruppe sind;
    b unabhängig bei jedem Auftreten eine ganze Zahl im Bereich von 0-3 ist; und
    c unabhängig bei jedem Auftreten eine ganze Zahl im Bereich von 0-2 ist.
  10. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten der Formel III aufweist
    Figure imgb0052
  11. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten der Formel IV aufweist
    Figure imgb0053
     worin x+y=100.
  12. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten aufweist, die abgeleitet sind von
    Figure imgb0054
  13. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten aufweist, die abgeleitet sind von
    Figure imgb0055
  14. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten aufweist, die abgeleitet sind von
    Figure imgb0056
  15. Optoelektronische Vorrichtung nach Anspruch 8, wobei das Polymer Struktureinheiten aufweist, die abgeleitet sind von
    Figure imgb0057
     und
    Figure imgb0058
  16. Optoelektronische Vorrichtung nach Anspruch 8, wobei sich Ar2 von einem Dibrom-9,9-dioctyl-fluoren-Monomer ableitet.
  17. Optoelektronische Vorrichtung nach Anspruch 8, wobei L von Phenylisochinolin abgeleitet ist.
  18. Optoelektronische Vorrichtung nach Anspruch 8, die mehr als eine Lichtemissionsschicht aufweist, und wobei mindestens eine der mehr als einen Lichtemissionsschichten das Polymer aufweist.
EP10754636.8A 2009-11-10 2010-09-10 Polymer für ein optoelektronisches bauelement Active EP2499181B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12/615,748 US8512879B2 (en) 2009-11-10 2009-11-10 Polymer for optoelectronic device
PCT/US2010/048360 WO2011059553A1 (en) 2009-11-10 2010-09-10 Polymer for optoelectronic device

Publications (2)

Publication Number Publication Date
EP2499181A1 EP2499181A1 (de) 2012-09-19
EP2499181B1 true EP2499181B1 (de) 2020-05-13

Family

ID=43416337

Family Applications (1)

Application Number Title Priority Date Filing Date
EP10754636.8A Active EP2499181B1 (de) 2009-11-10 2010-09-10 Polymer für ein optoelektronisches bauelement

Country Status (7)

Country Link
US (1) US8512879B2 (de)
EP (1) EP2499181B1 (de)
JP (1) JP5856969B2 (de)
KR (1) KR101782662B1 (de)
CN (2) CN107022064B (de)
TW (1) TWI496809B (de)
WO (1) WO2011059553A1 (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8053536B2 (en) * 2008-12-05 2011-11-08 General Electric Company Functionalized polyfluorenes for use in optoelectronic devices
US8048956B2 (en) * 2008-12-05 2011-11-01 General Electric Company Functionalized polyfluorenes for use in optoelectronic devices
JP5670353B2 (ja) * 2009-02-27 2015-02-18 メルク パテント ゲーエムベーハー アルデヒド基を含むポリマー、このポリマーの反応および架橋、架橋ポリマー、このポリマー含むエレクトロルミネッセンスデバイス
US20110077373A1 (en) * 2009-09-29 2011-03-31 General Electric Company Polymer and optoelectronic device comprising the same
CN105330825B (zh) * 2015-11-01 2017-10-20 华南理工大学 一种侧链含吡啶的水/醇溶性共轭聚合物及其制备方法与应用
WO2017146083A1 (ja) * 2016-02-25 2017-08-31 住友化学株式会社 発光素子及び該発光素子に用いる高分子化合物
CN106449999A (zh) * 2016-09-21 2017-02-22 广西南宁荣威德新能源科技有限公司 一种新型环保宽光谱太阳能电池材料
US11495756B2 (en) 2019-05-07 2022-11-08 Universal Display Corporation Organic electroluminescent materials and devices
TWI805261B (zh) * 2022-03-09 2023-06-11 住華科技股份有限公司 著色感光性樹脂組成物、及應用其之光學元件和顯示裝置

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4769292A (en) * 1987-03-02 1988-09-06 Eastman Kodak Company Electroluminescent device with modified thin film luminescent zone
DE69412567T2 (de) * 1993-11-01 1999-02-04 Hodogaya Chemical Co., Ltd., Tokio/Tokyo Aminverbindung und sie enthaltende Elektrolumineszenzvorrichtung
JPH10338872A (ja) 1997-06-09 1998-12-22 Tdk Corp 色変換材料およびこれを用いた有機ｅｌカラーディスプレイ
JP4743968B2 (ja) 1999-01-15 2011-08-10 住友化学株式会社 半導体ポリマー電界効果トランジスタ
CA2360644A1 (en) * 1999-02-04 2000-08-10 The Dow Chemical Company Fluorene copolymers and devices made therefrom
SG92833A1 (en) * 2001-03-27 2002-11-19 Sumitomo Chemical Co Polymeric light emitting substance and polymer light emitting device using the same
US6916902B2 (en) 2002-12-19 2005-07-12 Dow Global Technologies Inc. Tricyclic arylamine containing polymers and electronic devices therefrom
WO2005010081A1 (en) * 2003-07-16 2005-02-03 Sumitomo Chemical Company, Limited Aromatic monomer-and conjugated polymer-metal complexes
GB0403322D0 (en) * 2004-02-14 2004-03-17 Elam T Ltd Electroluminescent materials and devices
DE102004032527A1 (de) * 2004-07-06 2006-02-02 Covion Organic Semiconductors Gmbh Elektrolumineszierende Polymere
US7830081B2 (en) 2006-03-22 2010-11-09 General Electric Company Optoelectronic devices with multilayered structures
JP5130660B2 (ja) * 2006-05-31 2013-01-30 住友化学株式会社 有機薄膜トランジスタ
US7608677B2 (en) 2006-07-28 2009-10-27 General Electric Company Method for preparing polymeric organic iridium compositions
US7691292B2 (en) 2006-07-28 2010-04-06 General Electric Company Organic iridium compositions and their use in electronic devices
JP5591713B2 (ja) * 2007-12-17 2014-09-17 ゼネラル・エレクトリック・カンパニイ 光電子デバイス用発光性ポリマー材料

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
TWI496809B (zh) 2015-08-21
CN107022064B (zh) 2020-05-08
EP2499181A1 (de) 2012-09-19
KR20120088835A (ko) 2012-08-08
US20110108807A1 (en) 2011-05-12
US8512879B2 (en) 2013-08-20
CN102686637A (zh) 2012-09-19
WO2011059553A1 (en) 2011-05-19
JP2013510223A (ja) 2013-03-21
CN107022064A (zh) 2017-08-08
TW201132670A (en) 2011-10-01
KR101782662B1 (ko) 2017-10-23
JP5856969B2 (ja) 2016-02-10

Similar Documents

Publication Publication Date Title
EP2499181B1 (de) Polymer für ein optoelektronisches bauelement
EP2291354B1 (de) Phenylpyridineinheiten enthaltende verbindung
US8039125B2 (en) Compound comprising phenyl pyridine units
EP2502289B1 (de) Verfahren zur herstellung eines in einer optoelektronischen vorrichtung verwendbaren materials, das materialund die vorrichtung
EP2385940B1 (de) 2,4,6-tri(heteroarylphenyl)pyridine und elektronentransportierende materialien, die diese enthalten
US8962157B2 (en) Electron-transporting materials
US7989476B2 (en) Electron-transporting materials and processes for making the same
EP2324038B1 (de) Phenylpyridineinheiten enthaltende verbindung
KR101231509B1 (ko) 전자 수송 중합체
US8865905B2 (en) Organic compounds
US20100270537A1 (en) Optoelectronic devices and organic compounds used therein
US20110077373A1 (en) Polymer and optoelectronic device comprising the same

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20120611

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20140306

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: BOE TECHNOLOGY GROUP CO., LTD.

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20200108

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602010064335

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1270186

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200615

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200814

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200914

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200813

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200913

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200813

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1270186

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200513

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602010064335

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20210216

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20200930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200910

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200930

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200930

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200910

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230630

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240919

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240814

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240813

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20240920

Year of fee payment: 15